Available Formats

• ACTIVE INGREDIENT

  PHENAZOPYRIDINE HYDROCHLORIDE   97.5 MG

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• PURPOSE

  PHENAZOPYRIDINE HYDROCHLORIDE                     URINARY ANALGESIC

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• WARNINGS

  DO NOT EXCEED RECOMMENDED DOSAGE

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• ASK DOCTOR

  ASK DOCTOR BEFORE USE
  
  IF YOU HAVE KIDNEY DISEASE
  
  ALLERGIES TO FOODS,PRESERVATIVES OR DYES
  
  HAD A HYPERSENSITIVE REACTION TO PHENAZOPYRIDINE

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• WHEN USING

  WHEN USING THIS PRODUCT
  
  STOMACH UPSET MAY OCCUR,TAKING THIS PRODUCT WITH OR AFTER MEALS MAY REDUCE STOMACH UPSET
  
  YOUR URINE WILL BECOME REDDISH ORANGE IN COLOR.THIS IS NOT HARMFUL,BUT CARE SHOULD BE TAKEN TO
  
  AVOID STAINING CLOTHING OR OTHER ITEMS.

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• STOP USE

  STOP USE AND ASK A DOCTOR
  
  IF YOUR SYMPTOMS LAST FOR MORE THAN 2 DAYS
  
  YOU SUSPECT YOU ARE HAVING AN ADVERSE REACTION TO THE MEDICATION

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• PREGNANCY OR BREAST FEEDING

  ASK A HEALTH PROFESSIONAL BEFORE USE

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• KEEP OUT OF REACH OF CHILDREN

  IN CASE OF OVERDOSE ,GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

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• INDICATIONS & USAGE

  Use; fast relief from urinary pain,burning,urgency and frequency associated with urinary tract infections.

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• INACTIVE INGREDIENT

  Lactose, magnesium silicate, magnesium stearate, microcrystalline cellulose,
  
  pharmaceutical glaze, and sodium starch glycolate.

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• DOSAGE & ADMINISTRATION

  Adults and Children 12 years of age and over; take 2 tablets 3 times daily with a full glass of water,with or after meals as needed.
  
  Children under 12 years of age; consult a doctor.
  
  Do not use for more than 2 days ( 12 tablets ) without consulting a Doctor.

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• INGREDIENTS AND APPEARANCE

  WALGREENS URINARY PAIN RELIEF MAXIMUM STRENGTH  phenazopyridine hydrochloride tablet

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0113 Route of Administration ORAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENAZOPYRIDINE HYDROCHLORIDE (UNII: 0EWG668W17) (PHENAZOPYRIDINE - UNII:K2J09EMJ52) PHENAZOPYRIDINE HYDROCHLORIDE 97.5 mg

  Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G)   MAGNESIUM SILICATE (UNII: 9B9691B2N9)   MAGNESIUM STEARATE (UNII: 70097M6I30)

  Product Characteristics Color red Score no score Shape ROUND Size 7mm Flavor Imprint Code 975 Contains

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0113-01 1 in 1 CARTON 1 NDC:0363-0113-12 12 in 1 BLISTER PACK

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/05/2010

  Labeler - Walgreens Co. (008965063)

  Registrant - Reese Pharmaceutical Co (004172052)

  Establishment
  Name	Address	ID/FEI	Business Operations
  Reese Pharmaceutical Co		004172052	relabel, repack

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